Canonical Allele Identifier: CA2483404568
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1572942164
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454331T>G , CM000663.2:g.207454331T>G GRCh38
NC_000001.10:g.207627676T>G , CM000663.1:g.207627676T>G GRCh37
NC_000001.9:g.205694299T>G NCBI36
NG_013006.1:g.5032T>G , LRG_348:g.5032T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1236T>G ENSP00000514493.1:n.-385+1236T>G
ENST00000367057.8:c.-88T>G MANE Select ENSP00000356024.3:n.-88T>G
ENST00000367057.7:c.-88T>G ENSP00000356024.3:n.-88T>G
ENST00000367058.7:c.-88T>G ENSP00000356025.3:n.-88T>G
ENST00000367059.3:c.-88T>G ENSP00000356026.3:n.-88T>G
NM_001006658.2:c.-88T>G , LRG_348t1:c.-88T>G NP_001006659.1:n.-88T>G
NM_001877.4:c.-88T>G NP_001868.2:n.-88T>G
NM_001006658.3:c.-88T>G MANE Select NP_001006659.1:n.-88T>G
NM_001877.5:c.-88T>G NP_001868.2:n.-88T>G
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